JP6666496B1 - Gas barrier laminate - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a gas barrier laminate excellent in gas barrier property. A gas barrier laminate having a laminated structure including a barrier layer, an inorganic layer, and a substrate in this order, wherein the barrier layer contains a water-soluble resin and a condensate of a metal alkoxide hydrolyzate, Oxygen permeability (B) of the gas barrier laminate measured under the conditions of temperature 40 ° C. and relative humidity 0% RH, with respect to oxygen permeability (A) of the gas barrier laminate measured under the condition of temperature 23 ° C. and relative humidity 0% RH Is 1.80 or less, and the oxygen permeability (B) is 1.00 (cc / (m 2 · day · atm)) or less. [Selection diagram] None

Description

  The present invention relates to a gas barrier laminate.

  Packaging materials for foods, pharmaceuticals, and the like are often required to have a performance (gas barrier property) of preventing the transmission of gases such as oxygen and water vapor in order to suppress deterioration of the contents. In order to achieve excellent gas barrier properties, various techniques have been proposed so far.

  For example, Patent Literature 1 discloses a gas barrier laminate having a laminate structure including a base material, an evaporation layer (first layer) made of an inorganic compound, and a barrier layer (second layer) formed of a coating agent in this order. The body is described (claim 1 etc.). In the example No. In 1, a coating agent obtained by mixing a solution of a hydrolyzate of tetraethoxysilane and a solution of polyvinyl alcohol is laminated with a base structure of polyethylene terephthalate / a deposited layer of silicon oxide (first layer). Gas barrier laminates have been produced by applying to a body and drying.

Japanese Patent Application Laid-Open No. Hei 7-16491

  In the field of packaging materials for foods, pharmaceuticals, and the like, there is a constant demand for improved gas barrier properties. The present invention has been made in view of such circumstances, and an object thereof is to provide a gas barrier laminate having excellent gas barrier properties.

The present invention that can achieve the above object is as follows.
[1] A gas barrier laminate having a laminated structure including a barrier layer, an inorganic layer, and a substrate in this order,
The barrier layer includes a condensate of a water-soluble resin and a metal alkoxide hydrolyzate,
The oxygen permeability (A) of the gas barrier laminate measured at the temperature of 40 ° C. and the relative humidity of 0% relative to the oxygen permeability (A) of the gas barrier laminate measured at the temperature of 23 ° C. and the relative humidity of 0% RH Is 1.80 or less and the oxygen permeability (B) is 1.00 (cc / (m ² · day · atm)) or less.
[2] The gas barrier laminate according to [1], wherein the content of the water-soluble resin in the barrier layer is 10 to 90% by weight based on the entire barrier layer.
[3] The above-mentioned [1] or [2], wherein the solid content of the metal oxide in the barrier layer calculated from the amount of the metal alkoxide is 10 to 400 parts by weight per 100 parts by weight of the water-soluble resin. Gas barrier laminate.
[4] The gas barrier laminate according to any one of [1] to [3], wherein the water-soluble resin is a water-soluble resin having a hydroxy group.
[5] The gas barrier laminate according to any one of [1] to [3], wherein the water-soluble resin is polyvinyl alcohol.
[6] Any one of the above-mentioned [1] to [5], wherein the condensate of the metal alkoxide hydrolyzate is a condensate of a tetraethoxysilane hydrolyzate and / or a triisopropoxyaluminum hydrolyzate. 3. The gas barrier laminate according to item 1.
[7] The gas barrier laminate according to any one of [1] to [6], wherein the thickness of the barrier layer is 0.01 to 5.0 μm.

  According to the present invention, a gas barrier laminate excellent in gas barrier properties can be obtained.

  The present invention relates to a gas barrier laminate having a laminated structure including a barrier layer, an inorganic layer, and a substrate in this order. The gas barrier laminate only needs to include the barrier layer, the inorganic layer, and the substrate in this order, and another layer may be present between the layers. Examples of other layers include an adhesive layer, a primer layer, and the like.

  Examples of the laminated structure include “barrier layer / inorganic layer / substrate”, “barrier layer / inorganic layer / primer layer / substrate”, “barrier layer / primer layer / inorganic layer / substrate”, and “barrier layer”. / Primer layer / inorganic layer / primer layer / substrate "and" barrier layer / inorganic layer / first substrate / adhesive layer / second substrate ". In the above embodiment, each of the layers and the substrate may be a single layer or two or more layers. In this specification, “barrier layer / inorganic layer” indicates a state in which the barrier layer and the inorganic layer are in direct contact. Other expressions have the same meaning.

  It is preferable that the laminated structure is formed only of the barrier layer, the inorganic layer, and the base material. That is, the gas barrier laminate includes a barrier layer, an inorganic layer, and a substrate, and a laminated structure in which the barrier layer, the inorganic layer, and the substrate are laminated in this order (ie, “barrier layer / inorganic layer / substrate”). It is preferable to have In this embodiment, the barrier layer, the inorganic layer, and the substrate may each be two or more layers, but each is preferably a single layer.

  The present invention is characterized in that the barrier layer contains a condensate of a water-soluble resin and a hydrolyzate of a metal alkoxide.

  The water-soluble resin may be only one kind or two or more kinds. Examples of the water-soluble resin include polyvinyl alcohol, polyvinyl pyrrolidone, starch, methyl cellulose, carboxymethyl cellulose, sodium alginate and the like. Among these, a water-soluble resin having a hydroxy group is preferable, and a water-soluble resin polyvinyl alcohol is preferable, from the viewpoint of good aggregation of the water-soluble resin and the condensate of the metal alkoxide hydrolyzate in the barrier layer.

  The weight average molecular weight of the water-soluble resin is preferably from 10,000 to 100,000, more preferably from 12,000 to 90,000, and still more preferably from 14,000, from the viewpoint of gas barrier properties, flexibility and film forming properties. 80,000. This weight average molecular weight can be measured by gel permeation chromatography (GPC).

  When polyvinyl alcohol is used as the water-soluble resin, the average degree of polymerization is preferably from 100 to 3,000, more preferably from 200 to 2,500, and still more preferably from 400 to 2, from the viewpoint of gas barrier properties and flexibility. 000. The average degree of polymerization of polyvinyl alcohol can be calculated from the relative viscosity with water using a viscometer.

  When polyvinyl alcohol is used as the water-soluble resin, the degree of saponification is preferably 90 to 100 mol%, more preferably 95 to 100 mol%, and still more preferably 98 to 100 mol% from the viewpoint of gas barrier properties. The degree of saponification of polyvinyl alcohol can be determined by quantifying residual acetic acid groups in a sample using sodium hydroxide.

  The content of the water-soluble resin in the barrier layer is preferably from 10 to 90% by weight, more preferably from 15 to 65% by weight, and still more preferably from 20 to 60% by weight, from the viewpoint of gas barrier properties and flexibility. %. When two or more water-soluble resins are used, the content is the sum of the contents of the two or more water-soluble resins.

  The condensate of the metal alkoxide hydrolyzate may be only one kind or two or more kinds. Here, in the present invention, the “metal” of the “metal alkoxide” includes not only ordinary metals but also semimetals. Examples of the metal of the metal alkoxide include Si, Al, Ti, Zr and the like.

  The condensate of the metal alkoxide hydrolyzate is preferably a condensate of a tetraethoxysilane hydrolyzate and / or a condensate of a triisopropoxyaluminum hydrolyzate, more preferably a condensate of a tetraethoxysilane hydrolyzate. is there.

The solid content of the metal oxide in the barrier layer calculated from the amount of the metal alkoxide is preferably 10 to 400 parts by weight, more preferably 50 to 350 parts by weight, per 100 parts by weight of the water-soluble resin, from the viewpoint of gas barrier properties. Parts by weight, more preferably 70 to 300 parts by weight. Here, when the condensate of the metal alkoxide hydrolyzate is, for example, a condensate of a tetraethoxysilane hydrolyzate, the `` solid content in the barrier layer of the metal oxide calculated from the amount of the metal alkoxide '' is It means “solid content in the SiO ₂ barrier layer calculated from the amount of tetraethoxysilane”. The same applies to condensates of other metal alkoxide hydrolysates.

Further, when the condensate of the metal alkoxide hydrolyzate is, for example, a condensate of a tetraethoxysilane hydrolyzate and a condensate of triisopropoxyaluminum hydrolyzate, the `` metal oxide converted from the metal alkoxide amount '' The “solid content in the barrier layer” means “solid content in the SiO ₂ barrier layer calculated from the amount of tetraethoxysilane and solid content in the Al ₂ O ₃ barrier layer calculated from the content of aluminum triisopropoxy. Minutes ". The same applies when a condensate of another two or more metal alkoxide hydrolysates is present in the barrier layer.

  The barrier layer may contain another component different from the above-mentioned condensate of the water-soluble resin and the metal alkoxide hydrolyzate. Other components include, for example, components (eg, a solvent, a metal alkoxide and / or a hydrolyzate thereof) contained in a coating agent used for forming a barrier layer. From the viewpoint of gas barrier properties, the content of other components in the barrier layer is preferably 0 to 50% by weight, more preferably 0 to 30% by weight, and still more preferably 0 to 20% by weight, based on the entire barrier layer. . When two or more other components are present in the barrier layer, the content is the sum of the contents of the two or more other components.

The present invention relates to a gas barrier laminate having an oxygen permeability (A) (hereinafter sometimes abbreviated as “oxygen permeability (A)”) of 40 ° C. measured at a temperature of 23 ° C. and a relative humidity of 0% RH. And a ratio of oxygen permeability (B) (hereinafter sometimes abbreviated as “oxygen permeability (B)”) of the gas barrier laminate measured under the condition of relative humidity 0% RH (hereinafter “oxygen permeability (B) / Oxygen permeability (A) "is 1.80 or less. The oxygen permeability (A) and oxygen permeability (B) are both used the value calculated by the measurement method based on JIS ^{K7126-2 -2006.} In addition, the units of the oxygen permeability (A) and the oxygen permeability (B) when calculating the ratio are both “cc / (m ² · day · atm)”. Oxygen permeability (B) / oxygen permeability (A) is preferably 1.77 or less, more preferably 1.74 or less.

One of the features of the present invention is that the oxygen permeability (B) is 1.00 (cc / (m ² · day · atm)) or less. The oxygen permeability (B) is preferably 0.95 (cc / (m ² · day · atm)) or less, more preferably 0.90 (cc / (m ² · day · atm)) or less.

  The oxygen permeability (B) itself and the oxygen permeability (B) / oxygen permeability (A) described above are indicators of the cohesion of the water-soluble resin in the barrier layer and the condensate of the metal alkoxide hydrolyzate. Presumed. Specifically, the molecular motion of the condensate of the water-soluble resin and the metal alkoxide hydrolyzate in the barrier layer is increased at the temperature of 40 ° C. as compared with the condition of the temperature of 23 ° C., and as a result, the cohesive force between them is increased. It is estimated that the oxygen permeability (B) itself and the oxygen permeability (B) / oxygen permeability (A) increase in the barrier layer having a small value. Therefore, the gas barrier layer laminate having a small oxygen permeability (B) itself and a small oxygen permeability (B) / oxygen permeability (A) has a high cohesive force between a water-soluble resin and a condensate of a metal alkoxide hydrolyzate, It is presumed to show excellent gas barrier properties (eg, low water vapor permeability). However, the present invention is not limited to such estimation.

The cohesive force of the above-described condensate of the water-soluble resin and the metal alkoxide hydrolyzate indicates that the cohesion between an oxygen atom and / or a nitrogen atom contained in the water-soluble resin and the hydroxy group of the condensate of the metal alkoxide hydrolyzate is Presumed to be affected by hydrogen bonding. It is presumed that this hydrogen bond can be adversely affected by anions other than OH ⁻ (eg, Cl ⁻ ) remaining in the barrier layer. Therefore, by reducing the amount of anions other than OH ⁻ in the barrier layer to reduce the adverse effect on the hydrogen bond, the cohesion between the water-soluble resin and the condensate of the metal alkoxide hydrolyzate is high, and the gas barrier property is reduced. It is estimated that an excellent barrier layer can be formed. However, the present invention is not limited to such estimation.

The above estimation is supported by comparison of Examples 1 to 3 and Comparative Example 1 described below. Specifically, in Examples 1 to 3 using a coating agent in which the amount of anions other than OH ⁻ was reduced by anion exchange treatment, the oxygen permeability (B) itself and the oxygen permeability (B) / oxygen permeability of the present invention were used. Comparative Example 1 using a coating agent that did not perform the anion exchange treatment, although a gas barrier laminate that satisfied the requirements of the degree (A) and exhibited excellent gas barrier properties (low water vapor permeability) could be manufactured. Failed to produce such a gas barrier laminate. Patent Document 1 discloses oxygen permeability (B) itself and oxygen permeability (B) / oxygen permeability (A), which are features of the present invention, and means for realizing these (for example, anion exchange). Treatment) is neither described nor suggested. Also, in Example No. No. 1 describes that a coating agent produced by simply mixing a solution of a hydrolyzate of tetraethoxysilane and the like without performing an anion exchange treatment was used. 1 corresponds to Comparative Example 1 described later.

  The thickness of the barrier layer is preferably 0.01 to 5.0 μm, more preferably 0.05 to 2.0 μm, and still more preferably 0.1 to 1.0 μm, from the viewpoint of gas barrier properties and flexibility. . When two or more barrier layers are present, the thickness is the total thickness of the barrier layers. The thickness of the undried coating film may be appropriately set so as to be a desired thickness of the barrier layer.

  The inorganic substance forming the inorganic substance layer may be only one kind or two or more kinds. Examples of the inorganic substance include a metal and an inorganic oxide. The metal may be only one kind or two or more kinds. Aluminum is preferred as the metal. The inorganic oxide may be only one kind or two or more kinds. Examples of the inorganic oxide include aluminum oxide, silicon oxide, and magnesium oxide. Aluminum oxide is preferable as the metal oxide because it is inexpensive. The inorganic layer is preferably a layer formed by vapor deposition.

  The inorganic substance forming the inorganic layer is preferably an inorganic oxide, more preferably at least one selected from the group consisting of aluminum oxide, silicon oxide and magnesium oxide, and further preferably aluminum oxide.

  The thickness of the inorganic layer is preferably 1 to 200 nm, more preferably 2 to 150 nm, and still more preferably 3 to 100 nm, from the viewpoint of gas barrier properties and flexibility. In the case where two or more inorganic layers are present, the thickness is the thickness of each inorganic layer.

  The substrate may be only one kind or two or more kinds. Examples of the substrate include polyesters such as polyethylene terephthalate and polyethylene naphthalate, polyolefins such as polyethylene and polypropylene, polystyrene, polyamide, polyvinyl chloride, polycarbonate, polyacrylonitrile, and polyimide. The substrate is preferably polyester, more preferably polyethylene terephthalate.

  The thickness of the substrate is preferably 5 to 50 μm, more preferably 7 to 40 μm, and still more preferably 9 to 30 μm, from the viewpoint of the productivity of the gas barrier laminate. When two or more substrates are present, the thickness is the thickness of each substrate.

The gas barrier laminate of the present invention produces (1) a mixture containing a water-soluble resin, a metal alkoxide and / or a hydrolyzate thereof, and a solvent, and (2) performs anion exchange treatment on the obtained mixture. OH ^- to produce a reduced coating an anion of non, a coating agent obtained (3), and an inorganic material layer, and a substrate, is applied to the laminate having a laminated structure comprising, in this order, then dried It can be manufactured by doing.

The anion exchange treatment can be performed by adding an anion exchange resin to a mixture containing a water-soluble resin, a metal alkoxide and / or a hydrolyzate thereof, and a solvent, and stirring the resulting mixture. The amount of anion exchange resin, can not be determined unconditionally because it depends on the performance of the anion exchange resin, OH in the mixture ^- may be sufficiently removed anions other than amounts anion exchange resin It is preferred to use The temperature at which the mixture containing the anion exchange resin is stirred is preferably 5 to 80 ° C, more preferably 10 to 50 ° C, and the stirring time is preferably 5 to 120 minutes, more preferably 5 to 90 minutes. It is.

  Examples of the anion exchange resin include a resin into which a functional group having an anion exchange ability is introduced. Anion exchange resins can be classified according to the basicity of the functional groups. Specifically, an anion exchange resin is a strongly basic anion exchange resin having a quaternary ammonium group or the like as a functional group, or a weak anion exchange resin having a primary amino group, a secondary amino group, a tertiary amino group or the like as a functional group. It can be classified as a basic anion exchange resin. Examples of the resin into which the functional group having anion exchange ability is introduced include a styrene resin, an acrylic resin, and a methacrylic resin. The anion exchange resin is classified into a gel type or a macroporous type depending on a difference in resin structure such as a degree of crosslinking and porosity. The anion exchange resin that can be used in the production of the coating agent is not particularly limited, and a general one can be used.

  Commercial products can be used as the anion exchange resin. Examples of commercially available products include "Duolite UP5000" and "Amberlite IRA400J" manufactured by Dow Chemical Company, and "Diaion SA10A" manufactured by Mitsubishi Chemical Corporation.

  In the production of the coating agent, a high-pressure dispersion treatment of a mixture containing a water-soluble resin, a metal alkoxide and / or a hydrolyzate thereof, and a solvent may be performed. The high-pressure dispersion treatment may be performed before or after the anion exchange treatment, but is preferably performed before the anion exchange treatment. The high-pressure dispersion treatment is preferably performed by applying a high pressure to the mixture and passing the mixture at high speed through a thin tube formed in a chamber of a high-pressure dispersion device.

A commercial product can be used as the high-pressure dispersion device. Examples of commercially available products include “Ultra-High Pressure Homogenizer M110-E / H” manufactured by Microfluidics Corporation, “Starburst” manufactured by Sugino Machine Co., and “Homogenizer” manufactured by Sanwa Engineering Co., Ltd. The pressure of the high-pressure dispersing treatment is preferably 10~2,500kgf / cm ^2, more preferably 100~2,000kgf / cm ^2. The temperature of the high-pressure dispersion treatment is preferably 5 to 50C, more preferably 7 to 45C. The diameter of the capillary through which the mixture passes is preferably 10-500 μm, more preferably 50-400 μm. The number of times of the high-pressure dispersion treatment is preferably 1 to 2 times.

  In the production of the coating agent, a cation exchange treatment of a mixture containing a water-soluble resin, a metal alkoxide and / or a hydrolyzate thereof, and a solvent may be performed. The cation exchange treatment may be performed before or after the anion exchange treatment, but is preferably performed after the anion exchange treatment.

The cation exchange treatment can be performed by adding a cation exchange resin to a mixture containing a water-soluble resin, a metal alkoxide and / or a hydrolyzate thereof, and a solvent, and stirring the resulting mixture. The amount of the cation exchange resin to be used cannot be unconditionally determined because it depends on the performance of the cation exchange resin and the like. However, the amount of the cation exchange resin that can sufficiently remove cations other than H ⁺ in the mixture is used. It is preferred to use The temperature at which the mixture containing the cation exchange resin is stirred is preferably 5 to 80 ° C, more preferably 10 to 50 ° C, and the stirring time is preferably 5 to 120 minutes, more preferably 5 to 90 minutes. It is.

  Examples of the cation exchange resin include a resin into which a functional group having a cation exchange ability is introduced. Cation exchange resins can be classified according to the acidic strength of the functional groups. Specifically, the cation exchange resin can be classified into a strongly acidic cation exchange resin having a sulfo group or the like as a functional group or a weakly acidic cation exchange resin having a carboxy group or the like as a functional group. Examples of the resin into which a functional group having a cation exchange ability is introduced include a styrene resin, an acrylic resin, and a methacrylic resin. Further, the cation exchange resin is classified into a gel type or a macroporous type depending on a difference in resin structure such as a degree of crosslinking and porosity. The cation exchange resin that can be used in the production of the coating agent is not particularly limited, and a general cation exchange resin can be used.

  Commercial products can be used as the cation exchange resin. Examples of commercially available products include "Duolite C255LFH" manufactured by Rohm and Haas, "Diaion SK1B" manufactured by Mitsubishi Chemical Corporation, and "Amberlite IR120B" manufactured by Dow Chemical Company.

  From the viewpoint of gas barrier properties, the content of the water-soluble resin in the coating agent is preferably 0.1 to 10% by weight, more preferably 0.2 to 5% by weight, and still more preferably 0.3% by weight, based on the entire coating agent. ３3% by weight. When two or more water-soluble resins are used, the content is the sum of the contents of the two or more water-soluble resins. The description of the other water-soluble resins is the same as described above.

  The metal alkoxide in the coating agent may be only one kind or two or more kinds. Further, the hydrolyzate of the metal alkoxide may be only one kind or two or more kinds. The metal alkoxide and / or the hydrolyzate thereof is preferably at least one selected from the group consisting of tetraethoxysilane, tetraethoxysilane hydrolyzate, triisopropoxyaluminum and triisopropoxyaluminum hydrolyzate, more preferably Is a tetraethoxysilane and / or a tetraethoxysilane hydrolyzate, more preferably a tetraethoxysilane hydrolyzate.

  The content of the metal alkoxide and / or the hydrolyzate thereof in the coating agent is appropriately determined so that the “solid content in the barrier layer of the metal oxide calculated from the amount of the metal alkoxide” is included in the above-described preferred range. It is preferable to set.

  The solvent may be only one kind or two or more kinds. Examples of the solvent include water; alcohol solvents such as methanol, ethanol, and isopropyl alcohol; ester solvents such as ethyl acetate and butyl acetate; and ketone solvents such as methyl ethyl ketone. The solvent is preferably a mixed solvent of water and an organic solvent, more preferably a mixed solvent of water and an alcohol solvent, and still more preferably a mixed solvent of water and isopropyl alcohol.

  The content of the solvent in the coating agent is preferably 80 to 99.8% by weight based on the whole coating agent in order to maintain the water-soluble resin and the metal alkoxide and / or the hydrolyzate thereof uniformly in the coating agent. %, More preferably 90 to 99.6% by weight, even more preferably 94 to 99.4% by weight. When two or more solvents are used, the content is the sum of the contents of the two or more solvents.

  When a mixed solvent of water and an organic solvent (more preferably, an alcohol solvent, and still more preferably, isopropyl alcohol) is used as a solvent, the water-soluble resin and the metal alkoxide and / or a hydrolyzate thereof are uniformly maintained in the coating agent. The amount of the organic solvent (more preferably an alcohol solvent, more preferably isopropyl alcohol) in the mixed solvent is preferably 1 to 100 parts by weight, more preferably 5 to 80 parts by weight, based on 100 parts by weight of water. More preferably, it is 10 to 70 parts by weight. When two or more organic solvents are used, the above amount is the sum of the amounts of the two or more organic solvents.

  The description of the inorganic layer and the substrate in the laminate to which the coating agent is applied is the same as described above. The laminate to which the coating agent is applied may include the inorganic layer and the base material in this order, for example, between the inorganic material layer and the base material, or on the inorganic layer, another layer exists. You may. Examples of other layers include an adhesive layer, a primer layer, and the like.

  Examples of the laminate structure of the laminate to which the coating agent is applied include “inorganic layer / substrate”, “inorganic layer / primer layer / substrate”, “primer layer / inorganic layer / substrate”, and “primer layer / inorganic substance”. Layer / primer layer / substrate "," inorganic layer / first substrate / adhesive layer / second substrate "and the like. In the above embodiment, each of the layers and the substrate may be a single layer or two or more layers.

  The method of applying the coating agent may be a batch method or a continuous method. Examples of the coating method include a gravure method such as a direct gravure method and a reverse gravure method, a roll coating method such as a two roll beat coating method and a bottom feed three reverse coating method, a doctor knife method, a die coating method, and a bar coating method. , A dipping method, a spray coating method, a curtain coating method, a spin coating method, a flexo coating method, a screen coating method, a method using a brush or a brush, and the like.

  The drying of the coating film formed by applying the coating agent is preferably performed by heating in order to form a condensate of the metal alkoxide hydrolyzate in the barrier layer. Heating can be performed using a drying oven or a heater. From the viewpoint of the removal of the solvent and the progress of the condensation reaction of the metal alkoxide and / or the hydrolyzate thereof, the drying temperature is preferably 50 to 150 ° C, more preferably 60 to 150 ° C, and further preferably 70 to 140 ° C. The drying time is preferably 0.1 to 120 seconds, more preferably 0.2 to 100 seconds, and still more preferably 0.5 to 70 seconds. Drying is preferably performed in an atmospheric atmosphere at normal pressure.

  The gas barrier laminate of the present invention is excellent in gas barrier properties, and if it is used as a packaging material for foods, pharmaceuticals, etc., it is possible to suppress their deterioration and extend their storage period. As a result, it is possible to reduce the amount of waste of foods, medicines and the like, and the gas barrier laminate of the present invention can contribute to resource saving.

  Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited by the following examples, and appropriately modified within a range that can conform to the above and the following points. It is, of course, possible to implement them, and all of them are included in the technical scope of the present invention.

Manufacture of gas barrier laminate
Example 1
(1) Production of coating agent 10.4 g of tetraethoxysilane and 89.6 g of 0.1N hydrochloric acid were mixed, and the resulting mixture was stirred for 30 minutes to hydrolyze the tetraethoxysilane, thereby containing tetraethoxysilane. solid SiO ₂ content converted from the amount (hereinafter referred to as "SiO ₂ solids") is the solution a to prepare a 3% by weight.

  Solution B was prepared by mixing 100.0 g of polyvinyl alcohol (“PVA-105” manufactured by Kuraray Co., average degree of polymerization: 500, degree of saponification: 98 to 99 mol%), 290.8 g of water, and 32.3 g of isopropyl alcohol. did.

The solution A and the solution B are mixed so that the weight ratio of the solution A: the solution B is 2: 3, and 6 parts by weight of the anion exchange resin (manufactured by Dow Chemical Company) is added to 100 parts by weight of the obtained mixture. "Duolite UP5000") was added, and the resulting mixture was stirred at room temperature for 10 minutes to perform anion exchange treatment. Thereafter, the mixture was passed through a filter to remove the anion exchange resin to obtain a coating agent. The content and solid content of each component with respect to the whole prepared coating agent are described below: polyvinyl alcohol content = 1.2% by weight, SiO ₂ solid content = 1.8% by weight, water content = 87. 0.3% by weight, content of isopropyl alcohol = 9.7% by weight. Further, the amount of isopropyl alcohol relative to 100 parts by weight of water was 11.1 parts by weight.

(2) Production of Gas Barrier Laminate The obtained coating agent was coated on an aluminum oxide vapor-deposited film (“Barrierox 1011HG” manufactured by Toray Film Processing Co., Ltd., base material: polyethylene terephthalate (PET), base material thickness: 12 μm, inorganic layer: (Thickness of aluminum oxide layer, inorganic layer: 5 to 7.5 nm) is applied by a bar coater, dried in a hot air oven at 120 ° C. for 1 minute, and laminated with barrier layer / inorganic layer / substrate A gas barrier laminate having a structure was manufactured (thickness of barrier layer: 0.3 μm). Note that the drying was performed under an atmospheric atmosphere at normal pressure.

The content of polyvinyl alcohol in the barrier layer was 40% by weight based on the entire barrier layer, and the solid content of the SiO ₂ barrier layer calculated from the amount of tetraethoxysilane was 150% by weight per 100 parts by weight of polyvinyl alcohol. Parts by weight.

Example 2
The solution A and the solution B are mixed so that the weight ratio of the solution A: the solution B is 2: 3, and the obtained mixture is subjected to a high-pressure dispersion treatment apparatus (Microfluidics) at a temperature of 30 ° C. and a pressure of 1250 kgf / cm ^2. Except that the mixture after the high-pressure dispersion was subjected to an anion exchange treatment in the same manner as in Example 1 by using a "high pressure homogenizer M110-E / H" manufactured by Corporation, and using a high-pressure dispersion once using a thin tube having a diameter of 100 μm. Produced a coating agent in the same manner as in Example 1. The obtained coating agent was applied to the aluminum oxide vapor-deposited film and dried in the same manner as in Example 1 to produce a gas barrier laminate having a laminate structure of barrier layer / inorganic layer / substrate.

Example 3
6 parts by weight of a cation exchange resin ("Duolite C255LFH" manufactured by Rohm and Haas Company) was added to 100 parts by weight of the coating agent obtained in Example 2, and the obtained mixture was added at room temperature for 10 hours. Cation exchange treatment was performed by stirring for minutes. Thereafter, the mixture was passed through a filter to remove the cation exchange resin, thereby producing a coating agent. The obtained coating agent was applied to the aluminum oxide vapor-deposited film and dried in the same manner as in Example 1 to produce a gas barrier laminate having a laminate structure of barrier layer / inorganic layer / substrate.

Comparative Example 1
A coating agent was produced in the same manner as in Example 1 except that anion exchange was not performed. The obtained coating agent was applied to the aluminum oxide vapor-deposited film and dried in the same manner as in Example 1 to produce a gas barrier laminate having a laminate structure of barrier layer / inorganic layer / substrate.

Evaluation of the gas barrier laminate (1) oxygen permeability of the oxygen permeability The gas barrier layered product, JIS ^{K7126-2 -2006} based on, at a temperature of 23 ° C. or 40 ° C. and a relative humidity of 0% RH, an oxygen permeability It was measured using a degree measuring device (“OX-TRANML” manufactured by MOCON). The results are shown in Table 1 below. In the following, the oxygen permeability (A) of the gas barrier laminate measured at the temperature of 23 ° C. and the relative humidity of 0% RH is measured as “(A)” and the temperature is 40 ° C. and the relative humidity is 0% RH. The oxygen permeability (B) of the resulting svarrier laminate is described as “(B)”, and the ratio of (B) to (A) is described as “(B) / (A)”.

(2) in accordance with the water vapor permeability JIS K7129 ^-2008 B method, using a water vapor transmission rate measurement device (MOCON Co., Ltd., "PERMATRAN-W 3/33"), at a temperature of 40 ° C. and a relative humidity of 90% RH, The water vapor permeability of the obtained gas barrier laminate was measured. The results are shown in Table 1 below.

As shown in Table 1, Examples 1 to (B) / (A) were 1.80 or less and (B) was 1.00 (cc / (m ² · day · atm)) or less. The gas barrier laminate of No. 3 had lower water vapor permeability and was excellent in gas barrier properties as compared with the gas barrier laminate of Comparative Example 1 which did not satisfy the above requirements.

  The gas barrier laminate of the present invention has excellent gas barrier properties and is useful, for example, as a packaging material for foods, pharmaceuticals, and the like.

Claims (7)

A barrier layer, an inorganic layer, and a base material, a gas barrier laminate having a laminated structure including in this order,
The barrier layer includes a condensate of a water-soluble resin and a metal alkoxide hydrolyzate,
The oxygen permeability (A) of the gas barrier laminate measured at the temperature of 40 ° C. and the relative humidity of 0% relative to the oxygen permeability (A) of the gas barrier laminate measured at the temperature of 23 ° C. and the relative humidity of 0% RH Is 1.80 or less and the oxygen permeability (B) is 1.00 (cc / (m ² · day · atm)) or less.   The gas barrier laminate according to claim 1, wherein the content of the water-soluble resin in the barrier layer is 10 to 90% by weight based on the entire barrier layer.   The gas barrier laminate according to claim 1, wherein the solid content of the metal oxide in the barrier layer calculated from the amount of the metal alkoxide is 10 to 400 parts by weight per 100 parts by weight of the water-soluble resin.   The gas barrier laminate according to any one of claims 1 to 3, wherein the water-soluble resin is a water-soluble resin having a hydroxy group.   The gas barrier laminate according to any one of claims 1 to 3, wherein the water-soluble resin is polyvinyl alcohol.   The gas barrier laminate according to any one of claims 1 to 5, wherein the condensate of the metal alkoxide hydrolyzate is a condensate of a tetraethoxysilane hydrolyzate and / or a condensate of a triisopropoxyaluminum hydrolyzate. .   The gas barrier laminate according to any one of claims 1 to 6, wherein the thickness of the barrier layer is 0.01 to 5.0 µm.